Colon Cancer: Gene >> OLIG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333337
Start	33027028:33027028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166C>T
AA Mutation	p.Arg56Cys(p.R56C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333337
Start	33026873:33026873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.11A>G
AA Mutation	p.Asp4Gly(p.D4G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333337
Start	33027358:33027358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333337
Start	33027270:33027270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529308616
CDS Mutation	c.408G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333337
Start	33027099:33027099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333337
Start	33027228:33027228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.366C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OLIG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333337
Start	33027241:33027241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379G>A
AA Mutation	p.Ala127Thr(p.A127T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript